Digital Integration Lead

ADR Application Development Resources, Inc.; Pavia; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading company in the Pharma sector seeks a freelance consultant for a remote role primarily focused on MES integration. The consultant will work closely with site teams, providing technical guidance and oversight while ensuring adherence to cGMP standards and best practices. Applicants should have robust experience in the Pharma Industry and MES systems.

Competenze

• Strong experience with MES & Automation systems.
• Understanding of cGMP requirements.
• Experience with URS / FRS generation.

Mansioni

• Provide technical guidance and support for MES integration.
• Manage MES integration pack, roadmap and deliverables.
• Facilitating Agile planning for MES integration.

Conoscenze

Pharma Industry experience

MES integration

Automation systems

Agile planning

Technical guidance

Descrizione del lavoro

REMOTE opening but prefer someone in Italy who speaks Italian

Length :

July 1 though Dec. 31 2025

This is a FREELANCE Consulting opening and you would be paid US dollars

Must have Pharma Industry experience.

If interested, please send your CV in English to my email address :

Job Description :

• Work closely with Site team responsible for manufacturing equipment to provide technical guidance and support in the integration of equipment for Manufacturing Execution System (MES).
• Responsible for the MES integration pack, roadmap and deliverables. Liaise with site engineering leads and automation engineers.
• Strong experience with MES & Automation systems.
• Facilitating and continuing regular Agile planning for MES integration
• Analysis and solving of technical issues related to the MES integration.
• Manage activities of URS / FRS generation, software configuration / coding and general oversight to the MES software documentation practices
• A thorough understanding of system cGMP requirements and demonstrable knowledge of computer system design and maintenance lifecycle in cGMP environments.
• Liaise where necessary with MES platform provider, engineering contractor, and equipment vendors on the lifecycle of document preparation, approval, coding, and delivery